Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP509530.RAGuD5VFDhiG_DaJt3wjkyQTBOXeUhRVEu7YBF3eL8qdk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP509530.RAGuD5VFDhiG_DaJt3wjkyQTBOXeUhRVEu7YBF3eL8qdk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP509530.RAGuD5VFDhiG_DaJt3wjkyQTBOXeUhRVEu7YBF3eL8qdk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP509530.RAGuD5VFDhiG_DaJt3wjkyQTBOXeUhRVEu7YBF3eL8qdk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP509530.RAGuD5VFDhiG_DaJt3wjkyQTBOXeUhRVEu7YBF3eL8qdk130_provenance.
- NP509530.RAGuD5VFDhiG_DaJt3wjkyQTBOXeUhRVEu7YBF3eL8qdk130_assertion wasGeneratedBy ECO_0000203 NP509530.RAGuD5VFDhiG_DaJt3wjkyQTBOXeUhRVEu7YBF3eL8qdk130_provenance.
- NP509530.RAGuD5VFDhiG_DaJt3wjkyQTBOXeUhRVEu7YBF3eL8qdk130_assertion wasDerivedFrom befree-20150227 NP509530.RAGuD5VFDhiG_DaJt3wjkyQTBOXeUhRVEu7YBF3eL8qdk130_provenance.
- NP509530.RAGuD5VFDhiG_DaJt3wjkyQTBOXeUhRVEu7YBF3eL8qdk130_assertion SIO_000772 16272056 NP509530.RAGuD5VFDhiG_DaJt3wjkyQTBOXeUhRVEu7YBF3eL8qdk130_provenance.
- NP509530.RAGuD5VFDhiG_DaJt3wjkyQTBOXeUhRVEu7YBF3eL8qdk130_assertion evidence source_evidence_literature NP509530.RAGuD5VFDhiG_DaJt3wjkyQTBOXeUhRVEu7YBF3eL8qdk130_provenance.
- NP509530.RAGuD5VFDhiG_DaJt3wjkyQTBOXeUhRVEu7YBF3eL8qdk130_assertion description "[Aiming towards an understanding of the molecular background of retinitis pigmentosa, this paper describes the phenotype of a Swedish family with a mutation in IMPDH1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP509530.RAGuD5VFDhiG_DaJt3wjkyQTBOXeUhRVEu7YBF3eL8qdk130_provenance.